pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures

Summary
Synonym
  • PAMDDFS
Definition
A lissencephaly that is characterized by progressive microcephaly associated with abnormal facial features, hypotonia, and variable global developmental delay with impaired intellectual development and that has_material_basis_in homozygous or compound heterozygous mutation in the TUBGCP2 gene on chromosome 10q26.
Super Class
lissencephaly
Disease Ontology
DOID:0081266
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
10844 TUBGCP2 tubulin gamma complex component 2

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024